Institut de Radioprotection et de Sûreté Nucléaire, Service de Recherche en Radiobiologie et en Médecine régénérative, Laboratoire de Radiobiologie des expositions Médicales, Fontenay-aux-Roses, France; Sorbonne Université, Collège Doctoral, Paris, France.
Institut de Radioprotection et de Sûreté Nucléaire, Service de Recherche en Radiobiologie et en Médecine régénérative, Laboratoire de Radiobiologie des expositions Médicales, Fontenay-aux-Roses, France.
Int J Radiat Oncol Biol Phys. 2019 Jun 1;104(2):279-290. doi: 10.1016/j.ijrobp.2019.01.081. Epub 2019 Jan 29.
Stereotactic body radiation therapy offers good lung local tumor control by the administration of a high dose per fraction in small volumes. Stereotactic body radiation therapy preclinical modeling is now possible, and our aim was to develop a model of focal irradiation of the mouse lung and to investigate the impact of conditional hypoxia-inducible factor 1α (HIF-1α) deletion in the endothelium on radiation-induced tissue damage.
The Small Animal Radiation Research Platform was used to create a mouse model of focal irradiation of the lung using arc therapy. HIF-1α conditional deletion was obtained by crossing mice expressing Cre recombinase under the endothelial promoter VE-cadherin (VECad-Cre mice) with HIF-1α floxed mice.
Lung stereotactic arc therapy allows thoracic wall sparing and long-term studies. However, isodose curves showed that neighboring organs received significant doses of radiation, as revealed by ipsilateral lung acute red hepatization and major gene expression level modifications. Conditional HIF-1α deletion reduced acute lung edema and tended to diminish neutrophil infiltrate, but it had no impact on long-term global tissue damage.
Arc therapy for focal high-dose irradiation of mouse lung is an efficient model for long-term studies. However, irradiation may have a strong impact on the structure and function of neighboring organs, which must be considered. HIF-1α conditional deletion has no beneficial impact on lung damage in this irradiation schedule.
立体定向体部放射治疗通过在小体积中给予高剂量的单次分割,为肺部局部肿瘤提供了良好的控制效果。现在已经可以对立体定向体部放射治疗进行临床前建模,我们的目的是开发一种小鼠肺部焦点照射模型,并研究内皮细胞条件性缺氧诱导因子 1α(HIF-1α)缺失对放射诱导的组织损伤的影响。
使用小动物放射治疗研究平台,采用弧形治疗方法创建肺部焦点照射的小鼠模型。通过将内皮细胞启动子 VE-cadherin(VECad-Cre 小鼠)下表达 Cre 重组酶的小鼠与 HIF-1α 基因敲除小鼠杂交,获得 HIF-1α 条件性缺失。
肺部立体定向弧形放射治疗可以保护胸壁并进行长期研究。然而,等剂量曲线显示,相邻器官接收到了大量的辐射剂量,这表现为同侧肺部急性肝样变和主要基因表达水平的改变。条件性 HIF-1α 缺失减少了急性肺水肿,并倾向于减少中性粒细胞浸润,但对长期的整体组织损伤没有影响。
用于小鼠肺部焦点高剂量照射的弧形治疗是一种进行长期研究的有效模型。然而,照射可能对相邻器官的结构和功能产生强烈影响,这一点必须加以考虑。在这种照射方案中,HIF-1α 条件性缺失对肺损伤没有有益的影响。